%0 Journal Article %A Nico Scheer %A Yury Kapelyukh %A Anja Rode %A Stefan Oswald %A Diana Busch %A Lesley A. McLaughlin %A De Lin %A Colin J. Henderson %A C. Roland Wolf %T Defining Human Pathways of Drug Metabolism In Vivo through the Development of a Multiple Humanized Mouse Model %D 2015 %R 10.1124/dmd.115.065656 %J Drug Metabolism and Disposition %P dmd.115.065656 %X Variability in drug pharmacokinetics is a major factor in defining drug efficacy and side-effects; there remains an urgent need, particularly with the growing use of polypharmacy, to obtain more informative experimental data predicting clinical outcomes. Major species differences in multiplicity, substrate specificity and regulation of enzymes from the cytochrome P450-dependent mono-oxygenase system play a critical role in drug metabolism. To develop an in vivo model for predicting human responses to drugs we generated a mouse where 31 P450 genes from the Cyp2c, Cyp2d, and Cyp3a gene families were exchanged for their relevant human counterparts. The model has been improved through additional humanization for the nuclear receptors CAR and PXR that control the expression of key drug metabolizing enzymes and transporters. In this most complex humanized mouse model reported to date, the P450s function as predicted and we illustrate how these mice can be applied to predict drug-drug interactions in man. %U https://dmd.aspetjournals.org/content/dmd/early/2015/08/11/dmd.115.065656.full.pdf